H63D homozygous mutation syndrome explained: Wilson’s disease insidious iron sibling.
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A homozygous mutation of the
A homozygous mutation of the HFE gene H63D rarely triggers hereditary hemochromatosis. Far more often, however, it causes "H63D syndrome," an insidious, dangerous and potentially fatal syndrome whose progression can only be slowed if it is properly diagnosed in time, says Dr. Alexander Bartels, a Belgian physician.
For more information, visit https://www.h63d-syndrome.org - The International HFE Gene H63D Research Consortium.
Email: [email protected]
For more information, visit https://www.h63d-syndrome.org - The International HFE Gene H63D Research Consortium.
Email: [email protected]
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در تاریخ 1401/11/29 منتشر شده
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